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Tawfeg Ben Omran

4

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Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders

2018 Journal of Inherited Metabolic Disease
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SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors

2015 European Journal of Human Genetics
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Molecular analysis of phenylalanine hydroxylase (PAH) gene from dried blood spots from Libyan phenylketonuria patients

2010
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